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Enantioselective Pd-catalyzed tandem allylic alkylation reaction using monodentate phosphoramidite ligands for the formal total synthesis of huperzine A

  • Stony Brook University

Research output: Contribution to journalArticlepeer-review

17 Scopus citations

Abstract

A small library of fine-tunable monodentate phosphoramidite (MPN) ligands was found useful in selecting a highly efficient chiral ligand for the enantioselective Pd-catalyzed tandem allylic alkylation reaction. The reaction gave a critical tricyclic key intermediate with high enantiopurity for the formal total synthesis of (-)-huperzine A, a Lycopodium alkaloid derived from the club moss Huperzia serrata that possesses potent inhibitory activity against acetylcholine esterase (ACHe).

Original languageEnglish
Pages (from-to)1062-1066
Number of pages5
JournalOrganic Chemistry Frontiers
Volume1
Issue number9
DOIs
StatePublished - Nov 1 2014

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